TransferMan® 4m
Catalogue number 5191000023, listed by Eppendorf AG, Germany, under Micromanipulators And Microinjectors, Assisted Reproduction. 3 manufacturers in China are registered for this product code.
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
Who Else Makes It
Concentrated in Guangdong (2), Hubei (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Wuhan Huchuang Union Technology Co., Ltd. | Wuhan | Hubei | Manufacturer | 8 |
| HUA YUE Medical Technology Co., Ltd. | Guangzhou | Guangdong | Manufacturer | 7 |
| Guangzhou Pinzhi Medical Device Co., Ltd. | Guangzhou | Guangdong | Manufacturer | 5 |
Record
| Listed by | Eppendorf AG, Germany |
|---|---|
| FDA product code | MQJ |
| Device type | Micromanipulators And Microinjectors, Assisted Reproduction |
| Device class | Class 2 |
| Regulation | 21 CFR 884.6150 |
| Record published | 2017-02-11 |
| Record revised | 2023-06-19 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
| Distribution end date | 2018-11-09 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 5191000023 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Integra 3 | Research Instruments Ltd | 22 |
| LifeGlobal® Micropipet | LifeGlobal Group, LLC | 20 |
| Hariomed | HUA YUE Medical Technology Co., Ltd. | 4 |
| RI Syringe | Research Instruments Ltd | 3 |
| MTK-1VM-O2 | Narishige Lifemed Co., Ltd. | 1 |
| SFG Micropipettor | Spectrum Fertility Group Inc. | 1 |
| MMO-202NDVM | Narishige Lifemed Co., Ltd. | 1 |
| CellTram® vario | Eppendorf AG | 1 |
| MTK-1VM-Z3 | Narishige Lifemed Co., Ltd. | 1 |
| MTK-1VM-O1 | Narishige Lifemed Co., Ltd. | 1 |
| IM-9CVM | Narishige Lifemed Co., Ltd. | 1 |
| MTK-1VM-N3 | Narishige Lifemed Co., Ltd. | 1 |
Showing 12 of 42. All products under Micromanipulators And Microinjectors, Assisted Reproduction
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K142207 | 2015-01-23 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.